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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT00399022
Other study ID # SHEBA-06-4360-JZ-CTIL
Secondary ID
Status Withdrawn
Phase N/A
First received November 13, 2006
Last updated January 28, 2008

Study information

Verified date January 2008
Source Sheba Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Interventional

Clinical Trial Summary

Testing the efficacy of the SNRI medication Duloxetine for treating OCD patients who did not respond to SSRI


Recruitment information / eligibility

Status Withdrawn
Enrollment 40
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- OCD as main diagnosis according to DSM-IV

- Age 18 to 65

- Men and women

- YBOCS score is 18 or more, or 12 or more in case of only obsessions

Exclusion Criteria:

- Patients treated with Duloxetine, currently or in the past

- Patients having comorbid schizophrenia or psychotic disorder or bipolar disorder Patients with substance abuse disorder in the last 6 months Patients who were suicidal or did serious suicide attempt in the last year Pregnant or lactating women, or woman of childbearing potential, which is not using adequate contraception Patients with neurologic disturbance or disorder Patients with serious or imbalanced medical condition Patients with allergic response to SSRI or duloxetine Patients who started new treatment (CBT or pharmacology) in less than 3 months

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Duloxetine


Locations

Country Name City State
Israel Chaim Sheba Medical Center Ramat-Gan

Sponsors (1)

Lead Sponsor Collaborator
Sheba Medical Center

Country where clinical trial is conducted

Israel, 

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